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通过细胞壁多糖类型与受体结合蛋白之间的结合研究进行乳球菌噬菌体-宿主谱分析。

Lactococcal phage-host profiling through binding studies between cell wall polysaccharide types and receptor-binding proteins.

作者信息

White Kelsey, Eraclio Giovanni, McDonnell Brian, Lugli Gabriele Andrea, Crowley Tadhg, Ventura Marco, Volonté Federica, Cambillau Christian, Dal Bello Fabio, Mahony Jennifer, van Sinderen Douwe

机构信息

School of Microbiology, University College Cork, Cork, T12 Y337, Ireland.

APC Microbiome Ireland, University College Cork, Cork, T12 YT20, Ireland.

出版信息

Microb Genom. 2025 Apr;11(4). doi: 10.1099/mgen.0.001395.

DOI:10.1099/mgen.0.001395
PMID:40294100
Abstract

Dairy fermentations using mesophilic starter cultures rely on the activity of specific lactic acid bacteria (LAB) such as and for the acidification of milk. This biotechnological process can be affected by bacteriophage infection of LAB starter strains, which may result in delayed or even failed fermentations. Most studied lactococcal phages commence infection with the binding of a tail-associated receptor-binding protein (RBP) to a host cell surface-exposed cell wall polysaccharide (CWPS). In the present study, phage prevalence and diversity in whey samples originating from fermentations performed in various European countries employing undefined mesophilic starter cultures were investigated using phageome analysis. The range of RBP genotypes present in the phageomes and associated RBP-CWPS binding abilities were evaluated, resulting in the refinement and expansion of the RBP grouping system and the identification of several heretofore unknown RBP (sub)groups. These findings substantially expand our knowledge on lactococcal RBP diversity and their binding specificity towards CWPS receptor structures, thereby improving the predictability of fermentation outcomes and robustness of starter culture rotations and blends.

摘要

使用嗜温发酵剂培养物进行乳制品发酵依赖于特定乳酸菌(LAB)的活性,如 和 ,用于牛奶的酸化。这个生物技术过程可能会受到LAB发酵剂菌株噬菌体感染的影响,这可能导致发酵延迟甚至失败。大多数研究的乳球菌噬菌体通过尾部相关的受体结合蛋白(RBP)与宿主细胞表面暴露的细胞壁多糖(CWPS)结合开始感染。在本研究中,使用噬菌体组分析研究了来自欧洲不同国家采用未定义嗜温发酵剂培养物进行发酵的乳清样品中的噬菌体流行情况和多样性。评估了噬菌体组中存在的RBP基因型范围以及相关的RBP-CWPS结合能力,从而完善和扩展了RBP分组系统,并鉴定了几个迄今为止未知的RBP(亚)组。这些发现极大地扩展了我们对乳球菌RBP多样性及其对CWPS受体结构的结合特异性的认识,从而提高了发酵结果的可预测性以及发酵剂培养物轮换和混合的稳健性。

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本文引用的文献

1
Novel cell wall polysaccharide genotypes and structures of lactococcal strains isolated from milk and fermented foods.从牛奶和发酵食品中分离出的乳球菌的新型细胞壁多糖基因型和结构。
Int J Food Microbiol. 2024 Nov 2;424:110840. doi: 10.1016/j.ijfoodmicro.2024.110840. Epub 2024 Jul 31.
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Dynamics of the viral community on the surface of a French smear-ripened cheese during maturation and persistence across production years.在成熟过程中以及跨生产年份的保留期间,法国涂片成熟奶酪表面病毒群落的动态。
mSystems. 2024 Jul 23;9(7):e0020124. doi: 10.1128/msystems.00201-24. Epub 2024 Jun 11.
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Accurate structure prediction of biomolecular interactions with AlphaFold 3.
利用 AlphaFold 3 进行生物分子相互作用的精确结构预测。
Nature. 2024 Jun;630(8016):493-500. doi: 10.1038/s41586-024-07487-w. Epub 2024 May 8.
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A multifaceted investigation of lactococcal strain diversity in undefined mesophilic starter cultures.乳球菌菌株多样性的多方面研究,在未定义的中温发酵剂培养物中。
Appl Environ Microbiol. 2024 Mar 20;90(3):e0215223. doi: 10.1128/aem.02152-23. Epub 2024 Feb 9.
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A Metagenomics Approach to Enumerate Bacteriophages in a Food Niche.一种宏基因组学方法用于计数食品生境中的噬菌体。
Methods Mol Biol. 2024;2738:185-199. doi: 10.1007/978-1-0716-3549-0_12.
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Reduced synthesis of phospho-polysaccharide in Lactococcus as a strategy to evade phage infection.降低乳球菌中磷酸多糖的合成作为逃避噬菌体感染的策略。
Int J Food Microbiol. 2023 Dec 16;407:110415. doi: 10.1016/j.ijfoodmicro.2023.110415. Epub 2023 Sep 22.
7
Phables: from fragmented assemblies to high-quality bacteriophage genomes.噬菌体:从碎片化组装到高质量噬菌体基因组。
Bioinformatics. 2023 Oct 3;39(10). doi: 10.1093/bioinformatics/btad586.
8
The never-ending battle between lactic acid bacteria and their phages.乳酸菌与其噬菌体之间的永无止境的斗争。
FEMS Microbiol Rev. 2023 Jul 5;47(4). doi: 10.1093/femsre/fuad035.
9
Longitudinal Study of Phages in a Canadian Cheese Factory.加拿大奶酪厂噬菌体的纵向研究。
Appl Environ Microbiol. 2023 May 31;89(5):e0042123. doi: 10.1128/aem.00421-23. Epub 2023 Apr 19.
10
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Nat Methods. 2022 Jun;19(6):679-682. doi: 10.1038/s41592-022-01488-1. Epub 2022 May 30.